Department of Biochemistry and Biophysics, School of Medicine and Dentistry, University of Rochester, Rochester, NY, 14642, USA.
Center for RNA Biology, University of Rochester, Rochester, NY, 14642, USA.
Genome Biol. 2024 Jan 23;25(1):31. doi: 10.1186/s13059-023-03146-x.
In non-polarized cells, nonsense-mediated mRNA decay (NMD) generally begins during the translation of newly synthesized mRNAs after the mRNAs are exported to the cytoplasm. Binding of the FMRP translational repressor to UPF1 on NMD targets mainly inhibits NMD. However, in polarized cells like neurons, FMRP additionally localizes mRNAs to cellular projections. Here, we review the literature and evaluate available transcriptomic data to conclude that, in neurons, the translation of physiologic NMD targets bound by FMRP is partially inhibited until the mRNAs localize to projections. There, FMRP displacement in response to signaling induces a burst in protein synthesis followed by rapid mRNA decay.
在非极化细胞中,无意义介导的 mRNA 降解(NMD)通常在新合成的 mRNA 被输出到细胞质后开始翻译。FMRP 翻译抑制剂与 NMD 靶标上的 UPF1 的结合主要抑制 NMD。然而,在神经元等极化细胞中,FMRP 还将 mRNA 定位到细胞突起。在这里,我们回顾了文献并评估了可用的转录组数据,得出结论,在神经元中,与 FMRP 结合的生理 NMD 靶标的翻译被部分抑制,直到 mRNA 定位到突起。在那里,响应信号的 FMRP 位移会引起蛋白质合成的爆发,随后是快速的 mRNA 降解。